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IGF-1 LR3 Dosage: 20-50mcg/Day Chart + Calculator (2026)

IM hits one muscle, SubQ goes systemic — the route changes everything. 10-on/4-off protocol, bilateral splits, and reconstitution math.

Context first

Study findings do not automatically establish clinical benefit, safety, dosing, or suitability for an individual.

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Where These Numbers Come From

IGF-1 LR3 is a research tool and performance compound — it does not have human clinical trial data for the way it's used in the community.

IGF-1 induces muscle hypertrophy through satellite cell activation and increased protein synthesis in differentiated myofibers (Adams & McCue, 1998). LR3 IGF-1 infusion in animal models stimulates organ growth (adrenals, gut, kidneys, spleen) while suppressing endogenous IGF-1 and IGFBP levels (Bastian et al., 1993).

The LR3 modification provides a 20-30 hour half-life (vs minutes for native IGF-1), reduced IGFBP binding, and approximately 2-3x potency. Community doses of 20-80 mcg daily are extrapolated from animal research scaling, decades of bodybuilding experience, potency considerations, and risk management balancing anabolic effects against hypoglycemia (Florini et al., 1996).

Stacking Protocols

MK-677

20-40 mcg post-workout

12.5-25 mg PM

Growth stack

BPC-157

250-500 mcg

Growth + recovery

CJC-1295/Ipamorelin

20-30 mcg post-workout

CJC/Ipa

Per protocol

Comprehensive GH/IGF-1 axis

Community protocols describe running IGF-1 LR3 alone first and lowering LR3 doses to 20-30 mcg when stacking. Community sources emphasize watching blood sugar closely, since multiple compounds may compound hypoglycemia risk, and describe blood work (IGF-1, glucose, insulin, HbA1c) as essential.

Side Effects & Safety

Hypoglycemia (most immediate risk) — shaking, dizziness, sweating, confusion; community sources describe keeping fast-acting carbs available

Organ growth — gut distension and cardiomegaly possible with prolonged, high-dose use

Jaw and hand growth — subtle acromegaly-like changes with chronic use

Cancer risk — chronically elevated IGF-1 is associated with increased cancer risk in epidemiological studies

Joint pain — connective tissue changes, water retention

Fatigue/lethargy — common, especially initially

Injecting before sleep — community sources warn against this, as hypoglycemia during sleep is dangerous

mg to Units Conversion

On a standard 100-unit insulin syringe, each "unit" equals 0.01 mL (so 100 units = 1 mL). Once IGF-1 LR3 is reconstituted, the conversion from a target dose to syringe units depends on the chosen dilution.

The two reconstitution ratios most often described in community protocols are below.

Reconstitution A: 1 mg vial + 1 mL BAC water (1 mg/mL) — the standard dilution from the Quick Reference above.

25 mcg

0.025 mL

2.5 units

50 mcg

0.05 mL

5 units

75 mcg

0.075 mL

7.5 units

100 mcg

0.1 mL

10 units

Reconstitution B: 1 mg vial + 3 mL BAC water (333 mcg/mL) — more BAC water for larger, easier-to-measure draws.

0.15 mL

15 units

0.225 mL

22.5 units

0.3 mL

30 units

These conversions reflect the dilutions documented in community reconstitution protocols. They report how the math is described, not a recommended dosing schedule.

Core Supplies for This Protocol

The three essentials for running any reconstituted injectable: cold storage, accurate syringes, and metabolic tracking.

Cooluli Classic 4L Mini Fridge

Compact thermoelectric mini-fridge with heat/cool toggle. The most-mentioned dedicated peptide-storage fridge in research community sources — fits ~20 vials and runs quietly.

BD Ultra-Fine 31G 0.3cc 5/16" Insulin Syringes (Box of 90)

0.3cc 31G syringes — each gradation marks 1 unit (vs 2 units on 1cc), making sub-50-unit peptide doses accurate. BD Ultra-Fine is the most widely-cited brand in peptide community sources.

CONTOUR NEXT GEN Glucose Meter All-In-One Kit

Ascensia's CONTOUR NEXT GEN — the most clinically-validated home glucose meter. Includes 20 test strips + lancing device. Tracks the blood-sugar response GLP-1 users care about, especially during dose escalation.

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